Author :

Name  de la Chapelle A

4 Publications

First Author Title Year Journal Volume Pages
Aittomäki K Clinical features of primary ovarian failure caused by a point mutation in the follicle-stimulating hormone receptor gene. 1996 J Clin Endocrinol Metab 81 3722-6
Aittomäki K Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure. 1995 Cell 82 959-68
Fyfe JC The functional cobalamin (vitamin B12)-intrinsic factor receptor is a novel complex of cubilin and amnionless. 2004 Blood 103 1573-9
Clendenning M A frame-shift mutation of PMS2 is a widespread cause of Lynch syndrome. 2008 J Med Genet 45 340-5

To cite PlanMine, please refer to the following publication:

Rozanski, A., Moon, H., Brandl, H., Martín-Durán, J. M., Grohme, M., Hüttner, K., Bartscherer, K., Henry, I., & Rink, J. C.
PlanMine 3.0—improvements to a mineable resource of flatworm biology and biodiversity
Nucleic Acids Research, gky1070. doi:10.1093/nar/gky1070 (2018)